Evidence map›Paper›PMID 42818190›Full record

ArticlebioRxiv : the preprint server for biology2026

One-Dose Efficacy of Long-Acting Sorfequiline in a Mouse Model of Tuberculosis Preventive Therapy.

Si-Yang Li, James J Hobson, Nicole C Ammerman, Henry Pertinez, Jo Sharp, Nader Fotouhi, Steve Rannard, Andrew Owen, Eric L Nuermberger

Abstract readPreprint
In one paragraph

Article in bioRxiv : the preprint server for biology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

9 authors.

Si-Yang LiCenter for TB Research, Johns Hopkins University, Baltimore, Maryland, USA.
James J HobsonCentre for Excellence in Long-acting Therapeutics (CELT), University of Liverpool, Liverpool, UK.
Nicole C AmmermanCenter for TB Research, Johns Hopkins University, Baltimore, Maryland, USA.ORCID 0000-0001-9359-9144
Henry PertinezCentre for Excellence in Long-acting Therapeutics (CELT), University of Liverpool, Liverpool, UK.
Jo SharpCentre for Excellence in Long-acting Therapeutics (CELT), University of Liverpool, Liverpool, UK.
Nader FotouhiTB Alliance, New York, New York, USA.
Steve RannardCentre for Excellence in Long-acting Therapeutics (CELT), University of Liverpool, Liverpool, UK.ORCID 0000-0002-6946-1097
Andrew OwenCentre for Excellence in Long-acting Therapeutics (CELT), University of Liverpool, Liverpool, UK.
Eric L NuermbergerCenter for TB Research, Johns Hopkins University, Baltimore, Maryland, USA.ORCID 0000-0003-1440-9889

Funding

The Long-Acting/Extended Release Antiretroviral Resource Program (LEAP)R24AI118397 · NIAID · JOHNS HOPKINS UNIVERSITY · PI Charles W. Flexner · 2015 to 2026
$9.4M
Harnessing potent next-generation diarylquinolines for long-acting injectable formulations to prevent and treat tuberculosisR33AI161809 · NIAID · JOHNS HOPKINS UNIVERSITY · PI NUERMBERGER, ERIC L · 2024 to 2025
$1.8M
Harnessing potent next-generation diarylquinolines for long-acting injectable formulations to prevent and treat tuberculosisR61AI161809 · NIAID · JOHNS HOPKINS UNIVERSITY · PI NUERMBERGER, ERIC L · 2021 to 2023
$1.7M
NIAID NIH HHS R24 AI118397NIAID NIH HHS R33 AI161809NIAID NIH HHS R61 AI161809
6 · The paper itself

Abstract

Rationale: Tuberculosis preventive therapy (TPT) is essential for global tuberculosis control, yet estimated coverage remains well below global targets. Current World Health Organization (WHO)-recommended regimens require 1-9 months of treatment and are associated with suboptimal completion rates. Long-acting injectable (LAI) formulations offer the potential to improve TPT uptake and completion, with ideal products providing "one-and-done" options via a single administration. Sorfequiline, a second-generation diarylquinoline with superior potency over bedaquiline and lower QT prolongation risk, is a promising candidate for LAI TPT. Objectives: To experimentally determine exposure-activity relationships for sorfequiline as TPT, estimate target plasma exposures, and characterize the pharmacokinetics (PK), tolerability, and efficacy of sorfequiline LAI formulations. Methods: Oral sorfequiline dosing experiments established PK and pharmacodynamic relationships in a validated paucibacillary mouse model of TPT. Three candidate sorfequiline LAI formulations were evaluated for PK and tolerability in uninfected mice, followed by efficacy assessment compared to oral comparators (1HP, bedaquiline, sorfequiline). Measurement and Main Results: Oral dosing experiments established a provisional target plasma C Conclusion: Superior efficacy of a single-dose sorfequiline LAI injection compared to 1HP indicates the potential to meet the WHO target product profile for an optimal "one-and-done" LAI TPT clinical regimen.

Indexed as

Antibiotic ProphylaxisDiarylquinolinesDrug Delivery SystemsLatent TuberculosisMice, Inbred BALB/c

Identifiers

PMID42818190
PMCPMC13622149

What OpenQuestion holds

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Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.